Congenital adrenal hyperplasia with homozygous and heterozygous mutations: a rare family case report

Overview of attention for article published in BMC Endocrine Disorders, March 2022

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Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Cited by user Maxim Masiutin on 31 Oct 2023

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency, in all its forms, accounts for over 95% of diagnosed cases of congenital adrenal hyperplasia (CAH), and…

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